Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057518158

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057518158(A;A)
Make rs1057518158(A;C)
ReferenceGRCh38.p7 38.3/150
Chromosome4
Position5697612
GeneEVC2
is asnp
is mentioned by
dbSNPrs1057518158
dbSNP (old)rs1057518158
ClinGenrs1057518158
ebirs1057518158
HLIrs1057518158
Exacrs1057518158
Gnomadrs1057518158
Varsomers1057518158
Maprs1057518158
PheGenIrs1057518158
Biobankrs1057518158
1000 genomesrs1057518158
hgdprs1057518158
ensemblrs1057518158
gopubmedrs1057518158
geneviewrs1057518158
scholarrs1057518158
googlers1057518158
pharmgkbrs1057518158
gwascentralrs1057518158
openSNPrs1057518158
23andMers1057518158
23andMe allrs1057518158
SNPshotrs1057518158
SNPdbers1057518158
MSV3drs1057518158
GWAS Ctlgrs1057518158
Max Magnitude0
ClinVar
Risk rs1057518158(A;A)
Alt rs1057518158(A;A)
Reference Rs1057518158(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene EVC2
CLNDBN not provided
Reversed 1
HGVS NC_000004.11:g.5699339G>T
CLNSRC
CLNACC RCV000414626.1,